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DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease
Next-generation sequencing technologies made it possible to assay the effect of rare variants on complex diseases. As an extension of the “common disease-common variant” paradigm, rare variant studies are necessary to get a more complete insight into the genetic architecture of human traits. Associa...
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| Pubblicato in: | PLoS One |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5524342/ https://ncbi.nlm.nih.gov/pubmed/28742119 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0179364 |
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